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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929442Generated: November 1, 2026

N,N'-Dimethylethylenediamine → HCID 66790319, compound

https://huagongshe.com/reaction/1929442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-chlorotolueneHCID 609899—
Reactant7-Amino-2,2-dimethyl-2H-1,4-benzoxazin-3(4H)-oneHCID 13665546—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 66790319HCID 6679031939.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 7-amino-2,2-dimethyl-2H-1,4-benzoxazin-3(4H)-one (compound obtained in Reference Example 3(1); 150 mg), 5-bromo-2-chlorotoluene (321 mg), copper(I) iodide (37 mg), potassium carbonate (216 mg), N,N′-dimethylethylenediamine (40 μL) and toluene (8 mL) was heated at 110° C. overnight under argon atmosphere. After cooling, to the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel (solvent; n-hexane/ethyl acetate=4/1→1/1) to give 7-amino-4-(4-chloro-3-methylphenyl)-2,2-dimethyl-2H-1,4-benzoxazin-3(4H)-one (98 mg) as a pale orange powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188073B2
Source datasetuspto-grants-2012_05
ORD IDord-abc09fe762814c80b2fea48782bc874c
Source noteuspto-grants-2012_05